FDA Application
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NDC Search Results on Active Ingredient: acetaminophen
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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ASPIRIN; CAFFEINE; ACETAMINOPHEN | 66715-9749-3 | Lil' Drug Store Products, Inc. | NDA020802 | HUMAN OTC DRUG | NDA |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 0067-2039-24 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 0067-2039-07 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 0067-2039-84 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; ASPIRIN; CAFFEINE | 66715-6549-2 | Lil' Drug Store Products, Inc. | NDA020802 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; CAFFEINE; ASPIRIN | 52904-871-50 | Select Corporation | NDA020802 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; ASPIRIN; CAFFEINE | 0067-8201-03 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 69168-285-24 | Allegiant Health | NDA020802 | HUMAN OTC DRUG | NDA |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 0067-2035-16 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE | 21695-143-72 | Rebel Distributors Corp. | NDA021123 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 51662-1424-1 | HF Acquisition Co LLC, DBA HealthFirst | NDA022450 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 63323-434-00 | Fresenius Kabi USA, LLC | NDA204767 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 63323-434-41 | Fresenius Kabi USA, LLC | NDA204767 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 0264-4050-80 | B. Braun Medical Inc. | NDA204957 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 0264-4100-90 | B. Braun Medical Inc. | NDA204957 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 0264-4050-90 | B. Braun Medical Inc. | NDA204957 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 0143-9386-01 | Hikma Pharmaceuticals USA Inc. | NDA206968 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 0143-9386-10 | Hikma Pharmaceuticals USA Inc. | NDA206968 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE | 10702-340-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-343-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-341-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE | 10702-345-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-344-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-342-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 72260-129-01 | AFT Pharmaceuticals Ltd | NDA209471 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0145-72 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 0573-0147-90 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 0573-0147-09 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 0573-0147-36 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0145-99 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
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